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Fibroblast growth factor receptors and methods for their use

a growth factor receptor and fibroblast technology, applied in the field of fibroblast growth factor receptor 5 (fgfr5) polypeptides, to achieve the effect of decreasing fgfr5 gene expression and decreasing osteopontin gene expression

Inactive Publication Date: 2007-05-17
GENESIS RES & DEV
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Benefits of technology

"The present invention provides a new method for identifying and isolating fibroblast growth factor receptor 5 (FGFR5) polypeptides and polynucleotides. The invention also provides expression vectors and host cells transformed with these polynucleotides. Additionally, the invention provides binding agents that specifically bind to FGFR5 polypeptides and modulate their activity. The technical effects of the invention include the identification and isolation of new FGFR5 polypeptides and polynucleotides, as well as the development of new methods for detecting and modulating their activity."

Problems solved by technology

Such proteins may also be useful during tissue transplantation, where the body will often recognise the transplanted tissue as foreign and attempt to kill it, and also in bone marrow transplantation when there is a high risk of graft-versus-host disease in which the transplanted cells attack their host cells, often causing death.

Method used

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  • Fibroblast growth factor receptors and methods for their use
  • Fibroblast growth factor receptors and methods for their use
  • Fibroblast growth factor receptors and methods for their use

Examples

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example 1

Isolation of cDNA Sequences from Murine Lymph Node Stromal Cell Expression Libraries

[0156] The cDNA sequences of the present invention were obtained by high-throughput sequencing of cDNA expression libraries constructed from murine fsn- / - lymph node stromal cells as described below.

[0157] Lymph nodes were removed from flaky skin fsn- / - mice, the cells dissociated and the resulting single cell suspension placed in culture. After four passages, the cells were harvested. Total RNA, isolated using TRIzol Reagent (BRL Life Technologies, Gaithersburg, Md.), was used to obtain mRNA using a Poly(A) Quik mRNA isolation kit (Stratagene, La Jolla, Calif.), according to the manufacturer's specifications. A cDNA expression library (referred to as the MLSA library) was then prepared from the mRNA by Reverse Transcriptase synthesis using a Lambda ZAP Express cDNA library synthesis kit (Stratagene, La Jolla, Calif.). A second cDNA expression library, referred to as the MLSE library, was prepared ...

example 2

Characaterization of Isolated cDNA Sequences

[0159] The isolated cDNA sequences were compared to sequences in the EMBL DNA database using the computer algorithm BLASTN, and the corresponding polypeptide sequences (DNA translated to protein in each of 6 reading frames) were compared to sequences in the SwissProt database using the computer algorithm BLASTP. Specifically, comparisons of DNA sequences provided in SEQ ID NO: 1, 2-4 and 164 (isolated as described below) to sequences in the EMBL (Release 60, September 1999) DNA database, and the amino acid sequences correspoding to SEQ ID NO: 1-4 and 164 (provided in SEQ ID NO: 5-8, respectively) to sequences in the SwissProt and TrEMBL (up to October 20, 1999) databases were made as of Dec. 31, 1999. The cDNA sequences of SEQ ID NO: 1-4 and 164, and their corresponding polypeptide sequences (SEQ ID NO: 5-8, respectively) were determined to have less than 75% identity (determined as described above) to sequences in the EMBL and SwissProt ...

example 3

Isolation of Full Length cDNA Sequence of a Murine Fibroblast Growth Factor Receptor Homolog

[0162] The full-length cDNA sequence of a murine fibroblast growth factor receptor homolog was isolated as follows.

[0163] The MLSA cell cDNA library (described in Example 1) was screened with an [α32P]-dCTP labeled cDNA probe corresponding to nucleotides 1 to 451 of the coding region within SEQ ID NO: 1. Plaque lifts, hybridization and screening were performed using standard molecular biology techniques. The determined polynucleotide sequence of the full-length murine FGFR gene (referred to as muFGFR5β) is provided in SEQ ID NO: 2, with the corresponding polypeptide sequence being provided in SEQ ID NO: 6.

[0164] Analysis of the polynucleotide sequence of SEQ ID NO: 2 revealed the presence of a putative transmembrane domain encoded by nucleotides 1311 to 1370. The polypeptide sequence (SEQ ID NO: 6; FIG. 1) has regions similar to the extracellular domain of the fibroblast growth factor rece...

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Abstract

Isolated fibroblast growth factor receptor 5 (FGFR5) polypeptides are provided, together with polynucleotides encoding such polypeptides. Also provided are modulators of FGFR5 gene expression and binding molecules that specifically bind to, and agonize or antagonize, FGFR5 polypeptide finction. Binding molecules include antibodies, and functional fragments thereof, as well as scFv and Camelidae heavy chain IgG that specifically bind to FGFR5 thereby modulating the activity of FGFR5. Such binding agents and modulators of FGFR5 gene expression may be employed for the treatment of disorders including: osteopontin-mediated diseases; autoimmune diseases, such as systemic lupus erythematosus; bone disorders such as osteoporosis and osteopetrosis; and cancers, including cellular carcinomas such as hepatocellular carcinomas.

Description

CROSS-REFERENCE TO RELATED APPLICATIONS [0001] This application is a continuation-in-part of U.S. patent application Ser. No. 11 / 154,977, filed Jun. 15, 2005, which is a continuation-in-part of U.S. patent application Ser. No. 10 / 954,094, filed Sep. 29, 2004, which is a continuation-in-part of U.S. patent application Ser. No. 10 / 885,225, filed Jul. 6, 2004, which claims priority to U.S. provisional patent applications Nos. 60 / 484,877, filed Jul. 3, 2003; 60 / 513,171, filed Oct. 20, 2003; 60 / 562,155, filed Apr. 14, 2004; and 60 / 570,355, filed May 12, 2004. U.S. patent application Ser. No. 11 / 154,977 is also a continuation-in-part of U.S. patent application Ser. No. 10 / 613,413, filed Jul. 3, 2003, which is a continuation-in-part of U.S. patent application Ser. No. 10 / 157,444, filed May 28, 2002, now abandoned.REFERENCE TO SEQUENCE LISTING SUBMITTED ON COMPACT DISC [0002] This application incorporates by reference in its entirety the Sequence Listing contained in the accompanying two co...

Claims

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Application Information

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Patent Type & Authority Applications(United States)
IPC IPC(8): A61K39/395A61K48/00
CPCA61K38/177C07K14/71C12N15/1138C12N2310/11A61K38/00
Inventor MURISON, J. GREGCAO, ZHIHUI
Owner GENESIS RES & DEV
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